Job Summary
A company is looking for an Associate Director, Study Site Engagement to manage site engagement and support clinical trial operations remotely.
Key Responsibilities
- Facilitate effective partnerships between study teams, study sites, and CROs, including communication with Medical Affairs
- Support study teams in trial operations from feasibility through clinical study report within assigned regions
- Develop and maintain long-term strategic relationships with study sites and investigators to enhance engagement and recruitment
Required Qualifications
- Scientific degree (MD, PhD, MA/MS, BA/BS) in pharmaceutical science, chemistry, biology, or healthcare preferred
- 10+ years of experience in clinical research, with a focus on clinical trials
- Knowledge of clinical trial processes and regulations, including ICH-GCP
- Ability to work independently and collaboratively in a cross-functional, global environment
- Strong organizational, planning, and time management skills
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